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BDBM50484343 CHEMBL1835510

SMILES: Clc1ccc(OCCn2ccc(=O)[nH]c2=O)c(c1)C(=O)c1cc(Cl)cc(Cl)c1

InChI Key: InChIKey=LCJWQGQFJNCJIC-UHFFFAOYSA-N

Data: 1 KI

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50484343   
Target/Host
(Institution)		LigandTarget/Host
Links		Ligand
Links		Trg + Lig
Links		Ki
nM		ΔG°
kcal/mole		IC50
nM		Kd
nM		EC50/IC50
nM		koff
s-1		kon
M-1s-1		pHTemp
°C
Reverse transcriptase


(Human immunodeficiency virus 1)		BDBM50484343
PNG
(CHEMBL1835510)
Show SMILES Clc1ccc(OCCn2ccc(=O)[nH]c2=O)c(c1)C(=O)c1cc(Cl)cc(Cl)c1
Show InChI InChI=1S/C19H13Cl3N2O4/c20-12-1-2-16(28-6-5-24-4-3-17(25)23-19(24)27)15(10-12)18(26)11-7-13(21)9-14(22)8-11/h1-4,7-10H,5-6H2,(H,23,25,27)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
 820n/an/an/an/an/an/an/an/a



Volgograd State Medical University

Curated by ChEMBL


Assay Description
Inhibition of RNA-dependent DNA polymerase activity of HIV1 reverse transcriptase p66/p51 heterodimer using [8-3H]dGTP as substrate after 30 mins by ...

Bioorg Med Chem 19: 5794-802 (2011)


Article DOI: 10.1016/j.bmc.2011.08.025
BindingDB Entry DOI: 10.7270/Q2057JRG
More data for this
Ligand-Target Pair